Impact of Corpus Luteum Presence or Absence in the Incidence of Preeclampsia After Frozen Embryo Transfer

NCT04092829 | Terminated

• 1 other identifier: 1906-VLC-067-JB
• Study Type: interventional
• Target: 591
• Locations: 1 country
• Sites: 1

Brief Summary

Identifying modifiable factors that contribute to preeclampsia risk associated with assisted reproduction can improve maternal health. Recent studies have shown an increased risk for hypertensive disorders of pregnancy after in vitro fertilization, particularly for pregnancies occurring during a hormone replacement therapy such a donor egg recipient and a frozen embryo transfer. This risk may be partly attributable to the degree by which the assisted reproductive treatment affects the maternal hormonal environment, when the corpus luteum is a major source of reproductive hormones. On the other hand, cryopreserved embryos are usually thawed and replaced in in a natural or hormonally manipulated cycle; on this point, frozen embryo transfer is associated with better perinatal outcome regarding preterm birth and low birth weight yet higher risk of large for gestational age and macrosomia compared to fresh transfer. The objective of our study is to investigate whether the absence of corpus luteum adversely affects pregnancy and to analyse if there are differences in the perinatal outcomes due to differences in the endometrial preparation protocol for a frozen embryo transfer.

Conditions

Pre-Eclampsia; Frozen Embryo Transfer

Keywords

Pre-Eclampsia; Corpus Luteum; Frozen embryo transfer; Endometrial preparation

Outcome Measures

Primary Outcomes (1)

• Incidence of pre-eclampsia during pregnancy.

  Presence or absence of pre-eclampsia during pregnancy

  12 months

Secondary Outcomes (11)

• Bleeding during pregnancy

  12 months

• Hypertension during pregnancy

  12 months

• Eclampsia during pregnancy

  12 months

• Preeclampsia during pregnancy

  12 months

• Retarded intrauterine growth during pregnancy

  12 months

Study Arms (2)

FROZEN EMBRYO TRANSFER IN NATURAL CYCLE

NO INTERVENTION

After confirming ovarian rest (follicles \< 10 mm) with menstruation by means of vaginal ultrasound, an ultrasound control of the natural cycle will be carried out, inducing ovulation when an ovulatory follicle of size ≥ 17mm and an endometrium ≥ 7mm are found. Serum estradiol and progesterone values will be determined that day. This induction will be carried out with an ampoule of 250 μg of rHCG (Ovitrelle®). After the injection of Ovitrelle®, the administration of micronized vaginal progesterone (Progeffik® or Utrogestan®) 200 mg/ 12 hours and 7 days after the injection, thawing and transfer of a frozen euploid blastocyst will begin 48 hours later.

FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE

ACTIVE COMPARATOR

After confirming ovarian rest (follicles \< 10 mm) with menstruation by vaginal ultrasound, hormone replacement therapy with oestrogens (6 mg/day of oral oestradiol valerate - Progynova® or Progyluton®- or 150 ug/48 h of oestradiol in patches - Evopad®) will be started on day 2-3 of the cycle. On day 10-15 of treatment an ultrasound scan will be performed to assess endometrial growth and ovarian rest. After confirming an endometrial thickness ≥ 7mm by vaginal ultrasound, ovaries with follicles smaller than 10 mm, blood estradiol \>100 pg/ml and serum progesterone \< 1 ng/ml, luteal phase support will begin with the administration of 400 mg of micronized vaginal progesterone every 12 hours, a total of 10 shots, prior to embryo transfer of a thawed euploid blastocyst. same day. If the level of serum progesterone on the day of transfer is less than 9.2 ng/ml, a daily injection of subcutaneous progesterone (Prolutex®) will be added on the same day.

Procedure: FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE

Interventions

FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE PROCEDURE

The intervention group will be prepared with hormone replacement therapy with estrogens according to usual clinical practice. Frozen embryos will be transferred after ten doses of exogenous progesterone.

FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE

Eligibility Criteria

• Age: 18 Years - 44 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• All patients who, after IVF-PGT-A treatment with their own oocytes, present a euploid embryo for transfer.
• Transfer of a single euploid embryo

You may not qualify if:

• Moderate or high smoking (\> 5 cigarettes/day)
• BMI ≥30 kg/m2
• Chronic hypertension
• History of preeclampsia in previous pregnancies
• History of delayed uterine growth and placental insufficiency in previous pregnancies
• Use of donor sperm
• Woman's age ≥44 years
• Women with menstrual cycles longer than 35 days

Sponsors & Collaborators

• Instituto Valenciano de Infertilidad, IVI VALENCIA: lead
• IVI Bilbao: collaborator
• IVI Barcelona: collaborator
• IVI Madrid: collaborator
• Vida Recoletas Sevilla: collaborator
• IVI Vigo: collaborator
• IVI Roma: collaborator
• Hospital Universitario La Paz: collaborator
• IVI Mallorca: collaborator

Study Sites (1)

Ivi Valencia

Valencia, 46015, Spain

Location

MeSH Terms

Conditions

Pre-Eclampsia

Condition Hierarchy (Ancestors)

Hypertension, Pregnancy-Induced; Pregnancy Complications; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases

Study Officials

• JOSE BELLVER PRADAS, MDPhD

  IVIRMA VALENCIA

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Randomized prospective analysis.

Study Record Dates

• First Submitted: September 13, 2019
• First Posted: September 17, 2019
• Study Start: September 16, 2019
• Primary Completion: December 31, 2022
• Study Completion: December 31, 2022
• Last Updated: March 22, 2024

Record last verified: 2024-03

Locations

ES (1)